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N-(tert-Butoxycarbonyl)-L-cysteine methyl ester

Base Information Edit
  • Chemical Name:N-(tert-Butoxycarbonyl)-L-cysteine methyl ester
  • CAS No.:55757-46-5
  • Molecular Formula:C9H17NO4S
  • Molecular Weight:235.3
  • Hs Code.:2930909090
  • DSSTox Substance ID:DTXSID60450522
  • Nikkaji Number:J465.576A
  • Wikidata:Q82270293
  • Mol file:55757-46-5.mol
N-(tert-Butoxycarbonyl)-L-cysteine methyl ester

Synonyms:55757-46-5;N-(tert-Butoxycarbonyl)-L-cysteine methyl ester;n-boc-l-cysteine methyl ester;methyl (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-sulfanylpropanoate;Methyl (tert-butoxycarbonyl)-L-cysteinate;methyl (2R)-2-{[(tert-butoxy)carbonyl]amino}-3-sulfanylpropanoate;Boc-Cys-OMe;MFCD00799495;n-boc cysteine methyl ester;N-BOC-cysteine methyl ester;SCHEMBL295886;DTXSID60450522;NJGIAKIPSDCYAC-LURJTMIESA-N;L-Cysteine, N-[(1,1-dimethylethoxy)carbonyl]-, methyl ester;AM9652;AS-82965;tert-butoxycarbonyl-L-cysteine methyl ester;methyl N-(tert-butoxycarbonyl)-L-cysteinate;CS-0106046;N-(t-butoxycarbonyl)-l-cysteine methyl ester;E75395;N-(tert-Butoxycarbonyl)-l-cysteinemethyl ester;EN300-1273280;N-(tert-Butoxy-carbonyl)-L-cysteine methyl ester;N-(tert-Butoxycarbonyl)-L-cysteine methyl ester, 97%;N-[(1,1-dimethylethoxy)carbonyl]-L-cysteine, methyl ester

Suppliers and Price of N-(tert-Butoxycarbonyl)-L-cysteine methyl ester
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Sigma-Aldrich
  • N-(tert-Butoxycarbonyl)-L-cysteine methyl ester 97%
  • 25ml
  • $ 246.00
  • Sigma-Aldrich
  • N-(tert-Butoxycarbonyl)-L-cysteine methyl ester 97%
  • 5ml
  • $ 70.40
  • Chemenu
  • methyl(2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-sulfanylpropanoate 95%+
  • 25g
  • $ 552.00
  • American Custom Chemicals Corporation
  • N-(TERT-BUTOXYCARBONYL)-L-CYSTEINE METHYL ESTER 95.00%
  • 25ML
  • $ 1242.78
  • American Custom Chemicals Corporation
  • N-(TERT-BUTOXYCARBONYL)-L-CYSTEINE METHYL ESTER 95.00%
  • 5ML
  • $ 809.66
  • American Custom Chemicals Corporation
  • N-(TERT-BUTOXYCARBONYL)-L-CYSTEINE METHYL ESTER 95.00%
  • 1G
  • $ 761.00
  • AK Scientific
  • N-(tert-Butoxycarbonyl)-L-cysteine methyl ester
  • 1g
  • $ 144.00
  • AK Scientific
  • N-(tert-Butoxycarbonyl)-L-cysteine methyl ester
  • 2g
  • $ 185.00
  • AK Scientific
  • N-(tert-Butoxycarbonyl)-L-cysteine methyl ester
  • 10g
  • $ 414.00
  • Activate Scientific
  • N-Boc-L-Cysteine methyl ester 95% ee
  • 5 g
  • $ 512.00
Total 16 raw suppliers
Chemical Property of N-(tert-Butoxycarbonyl)-L-cysteine methyl ester Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Refractive Index:1.478 
  • Boiling Point:339.7°Cat760mmHg 
  • PKA:9.29±0.10(Predicted) 
  • Flash Point:159.2°C 
  • PSA:103.43000 
  • Density:1.134g/cm3 
  • LogP:1.37340 
  • XLogP3:1.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:6
  • Exact Mass:235.08782920
  • Heavy Atom Count:15
  • Complexity:237
Purity/Quality:

98%,99%, *data from raw suppliers

N-(tert-Butoxycarbonyl)-L-cysteine methyl ester 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)NC(CS)C(=O)OC
  • Isomeric SMILES:CC(C)(C)OC(=O)N[C@@H](CS)C(=O)OC
  • Uses N-(tert-Butoxycarbonyl)-L-cysteine methyl ester is a research chemical compound used in the preparation of terminal alkenes and allyl sulfides and preparation of trifluoromethyl substituted compounds.
Refernces Edit

Catalytic chain-breaking pyridinol antioxidants

10.1021/jo902226t

The study focuses on the synthesis and evaluation of 3-pyridinols, which are compounds carrying alkyltelluro, alkylseleno, and alkylthio groups, as potent antioxidant agents. These pyridinols were tested for their ability to inhibit azo-initiated peroxidation of linoleic acid in a water/chlorobenzene two-phase system and in a homogeneous phase. The chemicals used in the study include various 3-pyridinols with different substituents, N-acetylcysteine (NAC) as a water-soluble co-antioxidant, and N-tert-butoxycarbonyl cysteine methyl ester (LipCys), a lipid-soluble analogue of NAC. The purpose of these chemicals was to assess their antioxidant activity, specifically their capacity to quench peroxyl radicals, regenerate through reduction by thiol reducing agents, and their potential catalytic antioxidant behavior. The study aimed to understand the kinetic, thermodynamic, and mechanistic aspects of these antioxidants' activities and to identify the structural features that contribute to their high reactivity and effectiveness.

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